Triglycidyl isocyanurate

Base Information

• Chemical Name: Triglycidyl isocyanurate
• CAS No.: 2451-62-9
• Deprecated CAS: 414867-60-0
• Molecular Formula: C12H15 N3 O6
• Molecular Weight: 297.268
• Hs Code.: 2933.69
• European Community (EC) Number: 219-514-3
• ICSC Number: 1274
• NSC Number: 296964,296934
• DSSTox Substance ID: DTXSID4026262
• Nikkaji Number: J22.973C
• Wikidata: Q2453240
• Metabolomics Workbench ID: 144743
• ChEMBL ID: CHEMBL453863
• Mol file: 2451-62-9.mol

Synonyms:1,3,5-triglycidyl isocyanurate;1,3,5-triglycidyl-s-triazinetrione;alpha-1,3,5-triglycidyl-s-triazinetrione;alpha-TGT;NSC 296934;NSC-296934;Tepic;teroxirone;TGIC;triglycidyl isocyanurate

Chemical Property of Triglycidyl isocyanurate

Chemical Property:

• Appearance/Colour: white crystalline solid
• Vapor Pressure: 3.56E-10mmHg at 25°C
• Melting Point: 95-98 °C
• Refractive Index: 1.635
• Boiling Point: 501.1 °C at 760 mmHg
• PKA: -2.44±0.20(Predicted)
• Flash Point: 256.9 °C
• PSA: 103.59000
• Density: 1.625 g/cm³
• LogP: -2.63190
• Water Solubility.: <0.1 g/100 mL at 20℃
• XLogP3: -1.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 6
• Exact Mass: 297.09608521
• Heavy Atom Count: 21
• Complexity: 416

Purity/Quality:

99% ^*data from raw suppliers

Triglycidyl Isocyanurate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 46-23/25-41-43-48/22-52/53
• Safety Statements: 53-45-61

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Plastics & Rubber -> Epoxy Resins
• Canonical SMILES: C1C(O1)CN2C(=O)N(C(=O)N(C2=O)CC3CO3)CC4CO4
• Inhalation Risk: Evaporation at 20 °C is negligible; a harmful concentration of airborne particles can, however, be reached quickly when dispersed, especially if powdered.
• Effects of Short Term Exposure: The substance is severely irritating to the eyes. The substance may cause effects on the central nervous system, kidneys, liver, lungs and gastrointestinal tract. This may result in tissue lesions.
• Effects of Long Term Exposure: Repeated or prolonged contact may cause skin sensitization. May cause heritable genetic damage to human germ cells.
• Description: Occupational contact dermatitis can occur in people producing this chemical, in those producing the powder coat paint and in sprayers.
• Uses: 1,3,5-triglycidyl isocyanurate be used for curing agent of polyester and acrylic resin carboxyl-containing powder coating, manufacturing an electrical insulating laminates, adhesives, plastics stabilizers. TGIC is widely used as a cross-linking agent or curing agent in powder coating industry, It is used also in the printed circuit board industry, electrical insulation and as a stabilizer in plastic industry. Typical applications of polyester TGIC powder coatings are where sharp edges and corners exist such as on automotive wheels, air conditioners, lawn furniture, and air conditioner cabinets. Triglycidyl isocyanurate is used as cross-linker in heat-cured polyester paints, such as laminated sheetings, printed circuits, tools, inks, adhesives, lining materials etc.

Technology Process of Triglycidyl isocyanurate

There total 9 articles about Triglycidyl isocyanurate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.92%

1,3,5-tris-(3-chloro-2-hydroxy-propyl)-[1,3,5]triazinane-2,4,6-trione (7423-53-2) → teroxirone (2451-62-9,28825-96-9,240408-78-0)

Guidance literature:

With calcium oxide; at 50 - 60 ℃; for 4h;

Reference yield: 97.0%

→ teroxirone (2451-62-9,28825-96-9,240408-78-0)

Guidance literature:

Reference yield: 94.4%

C4H5NO2 → teroxirone (2451-62-9,28825-96-9,240408-78-0)

Guidance literature:

In methanol; at 4 ℃;

upstream raw materials:

cyanuric acid

epichlorohydrin

triallyl isocyanurate

1,3,5-tris-(3-chloro-2-hydroxy-propyl)-[1,3,5]triazinane-2,4,6-trione

Downstream raw materials:

anilazine

metaxalone

C₄₂H₆₀N₆O₉

C₄₂H₆₀N₆O₆

Refernces

• 1、 -. "Synthesis method of high-purity tris (glycidyl) isocyanurate". Paragraph 0027-0059. . Retrieved 2021/07/14.
• 2、 -. "Low-chlorine electronic-grade TGIC and preparation method thereof". Paragraph 0023-0046. . Retrieved 2021/08/21.